Data Paper
Cave morphology, microclimate and abundance of five cave predators from the Monte Albo
(Sardinia, Italy)
Enrico Lunghi , Claudia Corti , Manuela Mulargia, Yahui Zhao , Raoul Manenti , Gentile Francesco Ficetola , Michael Veith
‡ Key Laboratory of the Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, China
§ Museo di Storia Naturale dell'Università degli Studi di Firenze, "La Specola", Firenze, Italy
| Universität Trier Fachbereich VI Raum-und Umweltwissenschaften Biogeographie, Trier, Germany
¶ CEAS Santa Lucia, Siniscola, Italy
# Department of Environmental Sciences and Policy, Università degli Studi di Milano, Milano, Italy
¤ Université Grenoble Alpes, CNRS,, Grenoble, France
« LECA, Laboratoire d’Ecologie Alpine, Grenoble, France
» Université Savoie Mont Blanc, Annecy, France
Corresponding author: Enrico Lunghi (enrico.arti@gmail.com), Yahui Zhao (zhaoyh@ioz.ac.cn) Academic editor: Pedro Cardoso
Received: 20 Nov 2019 | Accepted: 16 Dec 2019 | Published: 03 Feb 2020
Citation: Lunghi E, Corti C, Mulargia M, Zhao Y, Manenti R, Ficetola GF, Veith M (2020) Cave morphology, microclimate and abundance of five cave predators from the Monte Albo (Sardinia, Italy). Biodiversity Data Journal 8: e48623. https://doi.org/10.3897/BDJ.8.e48623
Abstract
Background
Systematic data collection on species and their exploited environments is of key importance for conservation studies. Within the less-known environments, the subterranean ones are neither easy to be studied, nor to be explored. Subterranean environments house a wide number of specialised organisms, many of which show high sensitivity to habitat alteration. Despite the undeniable importance to monitor the status of the subterranean biodiversity, standardised methodologies to record biotic and abiotic data in these environments are still not fully adopted, impeding therefore the creation of
‡,§,| § ¶ ‡ #
#,¤,«,» |
© Lunghi E et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
comparable datasets useful for monitoring the ecological condition in the subterranean environments and for conservation assessment of related species.
New information
In this work we describe a methodology allowing the collection of standardised abiotic and biotic data in subterranean environments. To show this, we created a large dataset including information on environmental features (morphology and microclimate) and abundance of five predators (one salamander, three spiders and one snail) occurring in seven caves of the Monte Albo (Sardinia, Italy), an important biodiversity hotspot. We performed 77 surveys on 5,748 m of subterranean environments througout a year, recording 1,695 observations of the five cave predators. The fine-scale data collection adopted in our methodology allowed us to record detailed information related to both morphology and microclimate of the cave inner environment. Furthermore, this method allows us to account for species-imperfect detection when recording presence/abundance data.
Keywords
Dataset, standardised data collection, cave biology, troglophiles, salamander, spider, snail, monitoring, endangered species
Introduction
Subterranean environments represent peculiar habitats with an extraordinary biodiversity, including species with unique adaptive traits (Culver and Pipan 2015, Ficetola et al. 2019, Mammola 2019). Subterranean environments, ranging from small and narrow crevices to great and deep natural (or artificial) caves, are semi-closed systems with, at least, one connection with the surface (Culver and Pipan 2019). Thus, external climate influences the subterranean microclimate, in particular in its shallow parts (Badino 2004, Badino 2010, Culver and Pipan 2014). Subterranean environments are generally divided into different ecological zones according to the intensity of external influence (Culver and Pipan 2019);
this differentiation of microhabitats promotes local biodiversity (Campbell Grant et al. 2007, Culver and Pipan 2010). The entrance and twilight zones of the cave are the parts most influenced by the external climatic conditions, while, far from the surface, such influence becomes weaker and the microclimate is more stable (Lunghi et al. 2015, Culver and Pipan 2019).
Subterranean environments are inhabited by peculiar animal communities (Culver and White 2005, Romero 2009, Romero 2011). Species living in subterranean environments are subdivided into three macro-categories according to their degree of adaptation to the subterranean environment (Pavan 1944, Howarth and Moldovan 2018). The trogloxenes are species showing little or no adaptation and are often an accidental presence in
2
subterranean environments. Troglophiles are species that can show some adaptations to cave life and are able to spend at least part of their life in subterranean habitats.
Troglobites are obligate cave species showing the highest adaptation to these particular environments. Species commonly thought to visit caves accidentally were usually considered of least importance for subterranean habitats (Sket 2008, Trajano and de Carvalho 2017); however, recent studies showed that some of them are actually selecting areas with specific conditions (Lunghi et al. 2014, Manenti et al. 2017Lunghi et al. 2018a) and, in some cases, they can hold a key role in supplying organic matter to the entire ecosystem (Barzaghi et al. 2017, Culver and Pipan 2019). Most of the cave-related species are usually very sensitive to habitat alterations, a condition promoted by the high stability of the subterranean microclimate (Rizzo et al. 2015, Mammola et al. 2019a). The adaptation to the narrow range of environmental conditions present in these particular habitats, promotes a reduced home range and dispersal ability in subterranean organisms, often resulting in high rates of endemism (Manenti et al. 2018, Culver and Pipan 2019). This feature contributes to increasing the risk of extinction of cave animals (Williams et al. 2009, Lunghi et al. 2019) and thus, particular attention and updated information are needed to protect the subterranean environments and their inhabiting biodiversity (Ficetola et al.
2019, Mammola et al. 2019b).
Considering the complexity of exploring subterranean habitats (Zagmajster et al. 2010), information on these environments is generally limited to a small group of specialists and have coarse scales. For example, the information related to the cave inner morphology usually describes the overall shape of the subterranean space and it is often published in local speleological bulletins or cadasters. Moreover, studies on cave microclimate rarely focus on fine-scale data collection (Cigna 2002), which is the most reliable information to detect potential alterations of the environment due to human activities (Langer 2001, Marín et al. 2012, Mammola et al. 2019b), as well as to assess the microclimatic conditions actually experienced by species characterised by limited home ranges (Campbell Grant et al. 2007, Lunghi et al. 2017, Ficetola et al. 2018a, Mammola et al. 2018). Today, we observe a growing interest in the ecology and biodiversity of subterranean environments, as testified by the increasing amount of available literature (Romero 2009, Moldovan et al.
2018, Mammola 2019, White et al. 2019) and related datasets (Lunghi et al. 2018c, Lunghi et al. 2019b, Mammola et al. 2019c); however, a standardised methodology to record data in these environments is still not widely adopted, therefore impeding the creation of comparable datasets (Wynne et al. 2019). Here we provide a detailed description of a methodology useful to record fine-scale standardised biotic and abiotic data in subterranean environments. Using this approach, we produced a large dataset containing fine-scale data describing the morphology and microclimate of the inner environment from seven caves located in the Monte Albo massif (Sardinia, Italy) (Fig. 1). Furthermore, this approach also allowed us to record data on species presence and abundance, information of key importance for assessing species conservation status (Ficetola et al. 2017, Ficetola et al. 2018b).
General description
Purpose: The aim of this paper is to describe a standardised method to record fine-scale ecological and biological data in subterranean environments. To prove this, we here provide a large dataset recorded using the proposed approach (Suppl. material 1). The dataset includes morphological and microclimatic features from seven caves located in the Monte Albo massif (Sardinia, Italy). Furthermore, the dataset includes the abundance of five cave predators (Fig. 2): Hydromantes flavus Stefani, 1969 (Urodela: Plethodontidae), Meta bourneti (Roberts, 1995) (Araneae: Tetragnathidae), Metellina merianae (Scopoli, 1763) (Araneae: Tetragnathidae), Tegenaria sp. Latreille, 1804 (Araneae: Agelenidae), Oxychilus oppressus (Shuttleworth, 1877) (Gastropoda: Oxychilidae). Data here are integrated with those published in Lunghi (2018).
Additional information: Recommendations to adopt this survey method:
• This methodology was designed to monitor the endangered European cave salamanders of the genus Hydromantes (Ficetola et al. 2012, Lunghi et al. 2014, Lunghi et al. 2015), therefore the cave inner environment was divided according to the home range of these salamanders in subterranean environment (~3 m ; Lanza et al. 2006). Although this methodology is also useful to monitor a wide number of taxa, including frogs, toads, crickets, spiders and slugs/snails (Lunghi et al. 2017, Lunghi 2018, Lunghi et al. 2018a), we recommend to adapt the size of cave sectors based on the biology of the target species;
2 Figure 1.
Map of the study area showing the location of the Monte Albo and the seven monitored caves (pink circles). Detailed representation of the map is avoided to increase species protection (Lunghi et al. 2019).
a b
c d
e
Figure 2.
The five monitored predator species: a) the salamander Hydromantes flavus; b) the spider Metellina merianae; c) the spider Tegenaria sp.; d) the snail Oxychilus oppressus; e) the spider Meta bourneti.
a: Hydromantes flavus Stefani, 1969 (Urodela: Plethodontidae) b: Metellina merianae (Scopoli, 1763) (Araneae: Tetragnathidae) c: Tegenaria sp. Latreille, 1804 (Araneae: Agelenidae)
d: Oxychilus oppressus (Shuttleworth, 1877) (Gastropoda: Oxychilidae) e: Meta bourneti (Roberts 1995) (Araneae: Tetragnathidae)
• We here provide recommendation only on the length of cave sectors (i.e. 3 linear metres long), but not on the width. In our case, the inner cave environments did not reach a significant width (cave sector width always < 15 m and generally < 3 m); we therefore suggest to consider horizontally subdividing the cave sectors when the area is particularly wide;
• The species monitored here are generally found on cave walls and on the ground; if researchers need to also include the ceiling in their survey, we suggest to increase the searching time to 10 min per cave sector;
• The Visual Encounter Survey adopted here allows the collection of data only on species easily detectable by sight, while for those particularly secretive, alternative approaches are needed (Wynne et al. 2019);
• The easily detectability of our target species and the relatively small monitored area, allowed us to collect reliable data within the defined monitoring time; however, the time and/or cave sector size may be changed according to specific requirements.
Sampling methods
Study extent: We monitored 7 caves located in different areas of the Monte Albo massif (Fig. 1); surveys were performed at least twice per season (with a gap of 1 to 7 days between the two seasonal surveys), starting from Autumn 2015 to Summer 2016. We performed a total of 77 surveys (average ± SD per cave; 11.43 ± 4.39) throughout a year (Autumn, N = 14; Winter, N = 14; Spring, N = 35; Summer, N = 14). Each pair of surveys was performed by day (9 a.m. – 6 p.m.) and when similar meteorological conditions occurred (i.e. sunny days with similar air temperature and humidity). Each cave was divided into 3 longitudinal linear metres sections (hereafter, sectors) in order to collect fine- scale data of the inner environment (Ficetola et al. 2012, Lunghi et al. 2014). Overall, we monitored 179 cave sectors for a total of 5,748.35 m (ceilings were not considered as they were usually too high). For each cave, we measured the maximum height and width of the main entrance, while, at the end of each cave sector, we recorded: maximum height, maximum width and average wall irregularity (see Abiotic data collection – Morphology).
During each season, at 5-10 m from the cave entrance, we recorded the external air temperature and humidity. At the end of each cave sector, we seasonally recorded the following data: average air temperature, average air humidity, maximum and minimum illuminance (see Abiotic data collection – Microclimate). Within each sector, we recorded the abundance of five predator species (see Species data collection), providing a total of 1,695 observations: H. italicus, N = 831; M. bourneti, N = 182; M. merianae, N = 351;
Tegenaria sp., N = 151; O. oppressus, N = 180 (Fig. 2).
Sampling description: Abiotic data collection Morphology
Caves were explored entirely or up to the point reachable without speleological equipment.
Using a laser meter (Anself RZE-70, accuracy 2 mm), we recorded the maximum height
2
and width of the cave entrance (i.e. the main connection with the external environment).
Using a tape meter, the cave environment was divided into 3-metre cave sectors. At the end of each cave sector, we recorded the maximum height and width using a laser meter.
At the same point, we estimated the average maximum wall irregularity (i.e. presence of wall protuberances). To estimate wall irregularity, we used a string of one metre length, flattened vertically against the most irregular part of each cave wall (left and right), at a height ranging from 0.5 to 2 m; a tape meter was then used to measure the linear distance between the two extremities of the string (Ficetola et al. 2012, Lunghi et al. 2014). We then merged the data and obtained the average cave sector maximum wall irregularity.
Microclimate
During each season, air temperature and humidity were recorded in the external surroundings of each cave, in a shaded area 5-10 m from the entrance, using a Lafayette TDP92 thermo-hygrometer (accuracy: 0.1°C and 0.1%). At the end of each cave sector, the average air temperature and humidity were estimated by averaging data recorded at ground level and at 2.5 m height (or at the ceiling if sector height was lower). Microclimatic data were recorded paying attention to limit researcher influence (Lopes Ferreira et al.
2015). At the end of each sector, the maximum and minimum incident light was measured using a Velleman DVM1300 light meter (minimum recordable light: 0.1 lx).
Species data collection
Data on species occurrence and on the number of detected individuals were obtained using the Visual Encounter Survey (i.e. the surveyor visually inspected the whole cave sector without disturbing species) (Crump and Scott 1994). Within each cave sector, the surveyor dedicated 7.5 minutes in assessing the presence/abundance of the target species (Lunghi et al. 2015, Lunghi et al. 2017, Lunghi 2018); the use of a fixed time within each cave sector allows the surveyor to limit potential effects of imperfect species detection (Banks-Leite et al. 2014). When at least one individual was observed within the cave sector, the species was considered present; when no individuals were observed, the species was considered absent. For the three spiders, the number of cocoons observed per sector was also recorded.
Quality control: A dataset is provided to be readily used with R statistical software.
Several scientific studies support the reliability of the monitoring methodology proposed here (Ficetola et al. 2012, Ficetola et al. 2018a, Lunghi et al. 2014, Lunghi et al. 2015, Lunghi et al. 2017, Lunghi 2018, Lunghi et al. 2018a, Lunghi et al. 2018b).
The standardised methodology adpoted here and its overall repeatability, allowed the collection of comparable data from different environments during multiple time series (e.g.
seasons or years). This makes it possible to identify potential changes of the local environmental conditions, giving the chance to promptly plan habitat conservation actions (Langer 2001, Marín et al. 2012, Mammola et al. 2019b).
Species can be overlooked, especially the small-sized ones: a lack of observation does not mean a true absence (MacKenzie et al. 2006). Adopting a standardised monitoring method allows the limitation of biases due to imperfect species detection (Banks-Leite et al. 2014, Lunghi 2018); in our case, we standardised the effort (time/sector) dedicated in searching of species.
Sites were surveyed twice per season with a maximum gap ≤ 7 days, allowing us to meet prerequisites for population closure and to limit variation of climate conditions, which can, in turn, affect individuals’ activity (MacKenzie et al. 2006, Lunghi et al. 2015). The two seasonal presence/absence data collected within this short time allowed us to statistically estimate the probability to detect the target species. The seasonal pair of surveys performed here allowed us to estimate species detection probability for each season, providing, therefore, important information on species occurrence throughout the year.
Abundance data collected in a relatively short time allows us to estimate population size, thus providing the fundamental information to perform species conservation assessments (Ficetola et al. 2017, Ficetola et al. 2018b). The multiple counts of individuals can be analysed with the N-mixture models to estimate the population size; the higher the number of counts, the more precise the estimation will be (Ficetola et al. 2018b).
In order to consider possible differences in the activity of the studied species, surveys were performed during the four seasons. The studied species are usually more active at the end of the cold season (Bale and Hayward 2010, Lunghi et al. 2018b, Lunghi et al. 2018c), thus spring surveys were the most numerous. Increasing the number of surveys within a short period allows the increase of robustness of analyses related to detection probability and population size estimation (Banks-Leite et al. 2014, Ficetola et al. 2018b).
The target species are not obligate cave species and they likely show day/night changes in their activity pattern (Mammola and Isaia 2018); our methodology allowed us to avoid this potential bias. Species abundances obtained from each seasonal pair of survey can be merged to obtain an average seasonal species abundance; futhermore, the survey with the highest number of observations can be set as the maximum observed seasonal abundance.
The fine-scale standardised methodology described here allows us to characterise the multiple subterranean microhabitats (Campbell Grant et al. 2007) and collect detailed information on species abundance (Lunghi et al. 2015, Lunghi et al. 2017, Lunghi et al.
2018a, Lunghi 2018).
This methodology, based on just observations, is appropriate for monitoring protected species (Ficetola et al. 2016, Lunghi et al. 2016, Ficetola et al. 2017), providing a practical tool compatible with restrictions imposed by local and international law (Stoch and Genovesi 2016).
Geographic coverage
Description: The Monte Albo is listed as a Site of Community Importance (SCI) by European law (European Commission Habitats Directive 92/43/EEC), as it represents an important biodiversity hotspot including several endangered species (AA. VV. 2006, Mulargia et al. 2018); nonetheless, it also represents the whole distribution range of the Monte Albo cave salamander Hydromantes flavus (Lanza et al. 2006).
Coordinates: 40.4379 and 40.5701 Latitude; 9.5110 and 9.6815 Longitude.
Taxonomic coverage
Description: The presence and abundance of the following five cave predators were recorded: The Monte Albo cave salamander Hydromantes flavus, the spiders Meta bourneti, Metellina merianae and Tegenaria sp., the land snail Oxychilus oppressus (Fig.
2). Species identification of Tegenaria in the field is not possible without handling animals (Bolzern et al. 2013); to avoid disturbance, all records refer to the genus. The monitored species show different life traits (Lunghi et al. 2017, Lunghi 2018) and are at the top of the cave food chain, providing a top-down control to other cave-dwelling invertebrates;
however, interactions between these predator species are also possible (Pastorelli and Laghi 2006, Manenti et al. 2016, Lunghi et al. 2018c). The Monte Albo cave salamander is a local endemism that deserves particular protection, as its conservation status is considered Vulnerable by the IUCN Red List (Lanza et al. 2006, Lecis et al. 2009, Rondinini et al. 2013).
Temporal coverage
Data range: 2015-10-14 - 2016-6-27.
Usage rights
Use license: Creative Commons Public Domain Waiver (CC-Zero)
Data resources
Data package title: Dataset_Monte_Albo Number of data sets: 1
Data set name: data_monte_albo
Data format: Semi-colon delimited text file (.csv)
Description: Detailed information on cave features and abundance of five predator species (Suppl. material 1).
Column label Column description
country The name of the country in which the sampling was performed region The name of the region in which the sampling was performed county The name of the county in which the sampling was performed locationID The unique name of the surveyed location
eventDate The date in which the survey was performed eventSeason The season in which the survey was performed decimalLatitude Coordinates of the latitute in WGS84 decimal degrees (N) decimalLongitude Coordinates of the longitude in WGS84 decimal degrees (E) ElevationInMetres Elevation (m a.s.l.) of the surveyed site
entrance_heightValue The maximum height of the cave entrance (m) entrance_widthValue The maximum width of the cave entrance (m)
external_temperatureValue The outdoor air temperature (°C) measured at 5-10 m from the cave entrance
external_humidityValue The outdoor air humidity (%) measured at 5-10 m from the cave entrance
branchID The number of the cave branch
sector_depthValue The linear distance (m) of the sector from the cave entrance sector_heightValue The maximum height (m) of the cave sector
sector_widthValue The maximum width (m) of the cave sector
sector_wall_irregularityValue The average wall irregularity (m) of the cave sector. This value tends to 1 when cave walls show low irregularity, while it gets smaller when the wall irregularity increases
sector_temperatureValue The seasonal average air temperature (°C) of the cave sector sector_humidityValue The seasonal average air humidity (%) of the cave sector sector_max_illuminanceValue The seasonal average maximum illuminance (lx) of the cave sector sector_min_illuminanceValue The seasonal average minimum illuminance (lx) of the cave sector
Hydromantes_flavusQuantityType The typology of data recorded for Hydromantes flavus Stefani, 1969 (Urodela: Plethodontidae): individual
Hydromantes_flavusQuantity Number of observed Hydromantes flavus
Meta_bournetiQuantityType The typology of data recorded for Meta bourneti (Roberts 1995) (Araneae:
Tetragnathidae): individual
Meta_bournetiQuantity Number of observed Meta bourneti
Meta_bourneti_eggQuantityType The typology of data recorded for Meta bourneti egg sacks: cocoons Meta_bourneti_eggQuantity Number of observed Meta bourneti egg sacks
TegenariaQuantityType The typology of data recorded for Tegenaria Latreille, 1804 (Araneae:
Agelenidae): individual TegenariaQuantity Number of observed Tegenaria
Tegenaria_eggQuantityType The typology of data recorded for Tegenaria egg sacks: cocoons Tegenaria_eggQuantity Number of observed Tegenaria egg sacks
Metellina_merianaeQuantityType The typology of data recorded for Metellina merianae (Scopoli, 1763) (Araneae: Tetragnathidae): individual
Metellina_merianaeQuantity Number of observed Metellina merianae
Metellina_merianae_eggQuantityType The typology of data recorded for Metellina merianae egg sacks: cocoons Metellina_merianae_eggQuantity Number of observed Metellina merianae egg sacks
Oxychilus_oppressusQuantityType The typology of data recorded for Oxychilus oppressus (Shuttleworth, 1877) (Gastropoda: Oxychilidae): individual
Oxychilus_oppressusQuantity Number of observed Oxychilus oppressus
recordedBy The Name and Surname of person recording the data
Acknowledgements
Enrico Lunghi is supported by the Chinese Academy of Sciences President's International Fellowship Initiative for postdoctoral researchers, National Speleological Society and Instrumentl.
Author contributions
We thank P. Cardoso and S. Mammola for useful comments. E.L., M.M. R.M. and G.F.F.
participated in data collection; E.L. prepared tables, figures and first draft of the manuscript; M.V., R.M., G.F.F., Y.Z. and C.C contributed in reviewing the manuscript.
References
• AA. VV. (2006) Gestione del sito di importanza comunitaria "Monte Albo ITB021107".
POR Sardegna 2000-2006 ASSE I Misura 1.5 Rete Ecologica Regionale.
• Badino G (2004) Cave temperatures and global climatic change. International Journal of Speleology 33: 103‑114. https://doi.org/10.5038/1827-806X.33.1.10
• Badino G (2010) Underground meteorology - “what’s the weather underground?”. Acta Carsologica 39: 427‑448.
• Bale JS, Hayward SAL (2010) Insect overwintering in a changing climate. The Journal of Experimental Biology 213: 980‑994. https://doi.org/10.1242/jeb.037911
• Banks-Leite C, Pardini R, Boscolo D, Righetto Cassano C, Püttker T, Santos Barros C, Barlow J (2014) Assessing the utility of statistical adjustments for imperfect detection in tropical conservation science. Journal of Applied Ecology 51: 849‑859. https://doi.org/
10.1111/1365-2664.12272
• Barzaghi B, Ficetola GF, Pennati R, Manenti R (2017) Biphasic predators provide biomass subsidies in small freshwater habitats: a case study of spring and cave pools.
Freshwater Biology 62 (9): 1637‑1644. https://doi.org/10.1111/fwb.12975
• Bolzern A, Burckhardt D, Hänggi A (2013) Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data. Zoological Journal of the Linnean Society of London 168: 723‑848. https://doi.org/10.1111/zoj.12040
• Campbell Grant EH, Lowe WH, Fagan WF (2007) Living in the branches: population dynamics and ecological processes in dendritic networks. Ecology Letters 10: 165‑175.
https://doi.org/10.1111/j.1461-0248.2006.01007.x
• Cigna A (2002) Modern trend in cave monitoring. Acta Carsologica 31/1 (3): 35‑54.
• Crump ML, Scott NJ (1994) Visual encounter surveys. In: Heyer WR, Donnelly M., McDiarmid RW, Hayek LC, Foster MS (Eds) Measuring and monitoring biological diversity: standard methods for Amphibians.
• Culver DC, White WB (2005) Encyclopedia of caves. Elsevier Academic Press, San Diego, California, U.S.A..
• Culver DC, Pipan T (2010) Climate, abiotic factors, and the evolution of subterranean life. Acta Carsologica 39 (3): 577‑586.
• Culver DC, Pipan T (2014) Shallow subterranean habitats: Ecology, evolution, and conservation. Oxford University Press, New York, USA. https://doi.org/10.1093/
acprof:oso/9780199646173.001.0001
• Culver DC, Pipan T (2015) Shifting paradigms of the evolution of cave life. Acta Carsologica 44 (3): 415‑425. https://doi.org/10.3986/ac.v44i3.1688
• Culver DC, Pipan T (2019) The biology of caves and other subterranean habitats.
Second edition. New York https://doi.org/10.1093/oso/9780198820765.001.0001
• Ficetola GF, Pennati R, Manenti R (2012) Do cave salamanders occur randomly in cavities? An analysis with Hydromantes strinatii . Amphibia-Reptilia 33: 251‑259. https://
doi.org/10.1163/156853812X638536
• Ficetola GF, Lunghi E, Fiacchini D, Salvidio S (2016) Speleomantes ambrosii (Lanza, 1955) (Geotritone di Ambrosi), S. strinatii (Aellen, 1958) (Geotritone di Strinati). In:
Stoch F, Genovesi P (Eds) Manuali per il monitoraggio di specie e habitat di interesse comunitario (Direttiva 92/43/CEE) in Italia: specie animali. ISPRA, Serie Manuali e linee guida, 141/2016, Roma, 3 pp.
• Ficetola GF, Romano A, Salvidio S, Sindaco R (2017) Optimizing monitoring schemes to detect trends in abundance over broad scales. Animal Conservation 21: 221‑231.
https://doi.org/10.1111/acv.12356
• Ficetola GF, Lunghi E, Canedoli C, Padoa-Schioppa E, Pennati R, Manenti R (2018a) Differences between microhabitat and broad-scale patterns of niche evolution in
terrestrial salamanders. Scientific Reports 8: 10575. https://doi.org/10.1038/
s41598-018-28796-x
• Ficetola GF, Barzaghi B, Melotto A, Muraro M, Lunghi E, Canedoli C, Lo Parrino E, Nanni V, Silva-Rocha I, Urso A, Carretero MA, Salvi D, Scali S, Scarì G, Pennati R, Andreone F, Manenti R (2018b) N-mixture models reliably estimate the abundance of small vertebrates. Scientific Reports 8: 10357. https://doi.org/10.1038/
s41598-018-28432-8
• Ficetola GF, Canedoli C, Stock F (2019) The Racovitzan impediment and the hidden biodiversity of unexplored environments. Conservation Biology 33: 214‑216. https://
doi.org/10.1111/cobi.13179
• Howarth FG, Moldovan OT (2018) The ecological classification of cave animals and their adaptations. In: Moldovan OT, Kováč L, Halse S (Eds) Cave Ecology. Springer, Berlin, 26 pp. https://doi.org/10.1007/978-3-319-98852-8_4
• Langer WH (2001) Potential environmental impacts of quarrying stone in karst — A literature review. U.S. Geological Survey
• Lanza B, Pastorelli C, Laghi P, Cimmaruta R (2006) A review of systematics, taxonomy, genetics, biogeography and natural history of the genus Speleomantes Dubois, 1984 (Amphibia Caudata Plethodontidae). Atti del Museo Civico di Storia Naturale di Trieste 52: 5‑135.
• Lecis R, Andreone F, Edgar P, Corti C, Sindaco R, Romano A (2009) Speleomantes flavus. The IUCN Red List of Threatened Species 2009 https://doi.org/10.2305/
IUCN.UK.2009.RLTS.T20455A9200640.en
• Lopes Ferreira R, Mendes Martins V, Arantes Paixão E, Souza Silva M (2015) Spatial and temporal fluctuations of the abundance of Neotropical cave-dwelling moth Hypena sp. (Noctuidae, Lepidoptera) influenced by temperature and humidity. Subterranean Biology 16: 47‑60. https://doi.org/10.3897/subtbiol.16.5137
• Lunghi E, Manenti R, Ficetola GF (2014) Do cave features affect underground habitat exploitation by non-troglobite species? Acta Oecologica 55: 29‑35. https://doi.org/
10.1016/j.actao.2013.11.003
• Lunghi E, Manenti R, Ficetola GF (2015) Seasonal variation in microhabitat of salamanders: environmental variation or shift of habitat selection? PeerJ 3 https://
doi.org/10.7717/peerj.1122
• Lunghi E, Manenti R, Ficetola GF (2016) Speleomantes flavus (Stefani, 1969) (Geotritone del Monte Albo); S. genei (Temminck & Schlegel, 1838) (Geotritone di Gené); S. imperialis (Stefani, 1969) (Geotritone imperiale); S. sarrabusensis (Lanza et al., 2001) (Geotritone dei Sette Fratelli); S. supramontis (Lanza, Nascetti & Bullini, 1986) (Geotritone del Supramonte). In: Stoch F, Genovesi P (Eds) Manuali per il monitoraggio di specie e habitat di interesse comunitario (Direttiva 92/43/CEE) in Italia:
specie animali. ISPRA, Serie Manuali e linee guida, 141/2016, Roma, 3 pp.
• Lunghi E, Manenti R, Ficetola GF (2017) Cave features, seasonality and subterranean distribution of non-obligate cave dwellers. PeerJ 5 https://doi.org/10.7717/peerj.3169
• Lunghi E (2018) Ecology and life history of Meta bourneti (Araneae: Tetragnathidae) from Monte Albo (Sardinia, Italy). PeerJ 6 https://doi.org/10.7717/peerj.6049
• Lunghi E, Bruni G, Ficetola GF, Manenti R (2018a) Is the Italian stream frog (Rana italica Dubois, 1987) an opportunistic exploiter of cave twilight zone? Subterranean Biology 25: 49‑60. https://doi.org/10.3897/subtbiol.25.23803
• Lunghi E, Manenti R, Mulargia M, Veith M, Corti C, Ficetola GF (2018b) Environmental suitability models predict population density, performance and body condition for microendemic salamanders. Scientific Reports 8: 7527. https://doi.org/10.1038/
s41598-018-25704-1
• Lunghi E, Cianferoni F, Ceccolini F, Mulargia M, Cogoni R, Barzaghi B, Cornago L, Avitabile D, Veith M, Manenti R, Ficetola GF, Corti C (2018c) Field-recorded data on the diet of six species of European Hydromantes cave salamanders. Scientific Data 5 https://doi.org/10.1038/sdata.2018.83
• Lunghi E, Corti C, Manenti R, Ficetola GF (2019a) Consider species specialism when publishing datasets. Nature Ecology & Evolution 3 https://doi.org/10.1038/
s41559-019-0803-8
• Lunghi E, Zhao Y, Sun X, Zhao Y (2019b) Morphometrics of eight Chinese cavefish species. Scientific Data 6 https://doi.org/10.1038/s41597-019-0257-5
• MacKenzie DI, Nichols JD, Royle JA, Pollock KH, Bailey LL, Hines JE (2006) Occupancy estimation and modeling. Inferring patterns and dynamics of species occurrence. Academic Press, San Diego, California, U.S.A..
• Mammola S, Isaia M (2018) Day–night and seasonal variations of a subterranean invertebrate community in the twilight zone. Subterranean Biology 27: 31‑51. https://
doi.org/10.3897/subtbiol.27.28909
• Mammola S, Goodacre SL, Isaia M (2018) Climate change may drive cave spiders to extinction. Ecography 41: 233‑243. https://doi.org/10.1111/ecog.02902
• Mammola S (2019) Finding answers in the dark: caves as models in ecology fifty years after Poulson and White. Ecography 42 (7): 1331‑1351. https://doi.org/10.1111/ecog.
03905
• Mammola S, Piano E, Malard F, Vernon P, Isaia M (2019a) Extending Janzen's hypothesis to temperate regions: a test using subterranean ecosystems. Functional Ecology 33: 1638‑1650. https://doi.org/10.1111/1365-2435.13382
• Mammola S, Cardoso P, Culver DC, Deharveng L, Ferreira RL, Fišer C, Galassi DMP, Griebler C, Halse S, Humphreys WS, Isaia M, Malard F, Martinez A, Moldovan OT, Niemiller ML, Pavlek M, Reboleira ASPS, Souza-Silva M, Teeling EC, Wynne JJ, Zagmajster M (2019b) Scientists’ warning on the conservation of subterranean ecosystems. BioScience 69: 641‑650. https://doi.org/10.1093/biosci/biz064
• Mammola S, Cardoso P, Angyal D, Balázs G, Blick T, Brustel H, Carter J, Ćurčić S, Danflous S, Dányi L, Déjean S, Deltshev C, Elverici M, Fernández J, Gasparo F, Komnenov M, Komposch C, Kováč L, Boğaç Kunt K, Mock A, Moldovan O, Naumova M, Pavlek M, Prieto CE, Ribera C, Rozwałka R, Růžička V, Vargovitsh RS, Zaenker S, Isaia M (2019c) Continental data on cave-dwelling spider communities across Europe (Arachnida: Araneae). Biodiversity Data Journal 7: e38492. https://doi.org/10.3897/BDJ.
7.e38492
• Manenti R, Lunghi E, Canedoli C, Bonaccorsi M, Ficetola GF (2016) Parasitism of the leech, Batracobdella algira (Moquin-Tandon, 1846), on Sardinian cave salamanders (genus Hydromantes) (Caudata: plethodontidae). Herpetozoa 29 (1/2): 27‑35.
• Manenti R, Lunghi E, Ficetola GF (2017) Cave exploitation by an usual epigean species: a review on the current knowledge on fire salamander breeding in cave.
Biogeographia 32: 31‑46. https://doi.org/10.21426/B632136017
• Manenti R, Barzaghi B, Lana E, Stocchino GA, Manconi R, Lunghi E (2018) The stenoendemic cave-dwelling planarians (Platyhelminthes, Tricladida) of the Italian Alps
and Apennines: conservation issues. Journal of Nature Conservation 45: 90‑97. https://
doi.org/10.1016/j.jnc.2018.08.001
• Marín AI, Andreo B, Jiménez-Sánchez M, Domínguez-Cuesta MJ, MeléNdez-Asensio M (2012) Delineating protection areas for caves using contamination vulnerability mapping techniques: the case of Herrerías Cave, Asturias, Spain. Journal of Cave and Karst Studies 74 (1): 103‑115. https://doi.org/10.4311/2011jcks0197
• Moldovan OT, Kovác L, Halse S (2018) Cave Ecology. Springer Nature Switzerland https://doi.org/10.1007/978-3-319-98852-8
• Mulargia M, Corti C, Lunghi E (2018) The herpetofauna of the Monte Albo, Sardinia (Italy). Russian Journal of Herpetology 25 (3): 172‑176.
• Pastorelli C, Laghi P (2006) Predation of Speleomantes italicus (Amphibia: Caudata:
Plethodontidae) by Meta menardi (Arachnida: Araneae: Metidae). Atti del 6° Congresso Nazionale della Societas Herpetologica Italica (Roma, 27.IX-1.X.2006). Roma, 3 pp.
• Pavan M (1944) Appunti di biospeleologia I. Considerazioni sui concetti di Troglobio, Troglofilo e Troglosseno. Le Grotte d'Italia 5: 33‑41.
• Rizzo V, Sánchez-Fernández D, Fresneda J, Cieslak A, Ribera I (2015) Lack of evolutionary adjustment to ambient temperature in highly specialized cave beetles.
BMC Evolutionary Biology 15 https://doi.org/10.1186/s12862-015-0288-2
• Romero A (2009) Cave Biology. Cambridge University Press, Cambridge, UK. https://
doi.org/10.1017/CBO9780511596841
• Romero A (2011) The Evolution of Cave Life. American Scientist 99: 144‑151. https://
doi.org/10.1511/2011.89.144
• Rondinini C, Battistoni A, Peronace V, Teo li C (2013) Lista Rossa IUCN dei vertebrati Italiani. Comitato Italiano IUCN e Ministero dell’Ambiente e della Tutela del Territorio e del Mare
• Sket B (2008) Can we agree on an ecological classification of subterranean animals?
Journal of Natural History 42: 1549‑1563. https://doi.org/10.1080/00222930801995762
• Stoch F, Genovesi P (2016) Manuali per il monitoraggio di specie e habitat di interesse comunitario (Direttiva 92/43/CEE) in Italia: specie animali. ISPRA
• Trajano E, de Carvalho MR (2017) Towards a biologically meaningful classification of subterranean organisms: a critical analysis of the Schiner-Racovitza system from a historical perspective, difficulties of its application and implications for conservation.
Subterranean Biology 22: 1‑26. https://doi.org/10.3897/subtbiol.22.9759
• White W, Culver DC, Pipan T (2019) Encyclopedia of caves. Academic Press https://
doi.org/10.1016/B978-0-12-814124-3.09991-X
• Williams SE, Williams M, VanDerWal J, Isaac JL, Shoo LP, Johnson CN (2009)
Ecological specialization and population size in a biodiversity hotspot: How rare species avoid extinction. Proceedings of the National Academy of Sciences of the United States of America 106 (suppl. 2): 19737‑19741. https://doi.org/10.1073/pnas.0901640106
• Wynne JJ, Howarth FG, Sommer S, Dickson BG (2019) Fifty years of cave arthropod sampling: techniques and best practices. International Journal of Speleology 48 (1):
33‑48. https://doi.org/10.5038/1827-806X.48.1.2231
• Zagmajster M, Culver DC, Christman MC, Sket B (2010) Evaluating the sampling bias in pattern of subterranean species richness: combining approaches. Biodiversity and Conservation 19: 3035‑3048. https://doi.org/10.1007/s10531-010-9873-2
Supplementary material
Suppl. material 1: Dataset_Monte_Albo
Authors: Enrico Lunghi, Claudia Corti, Manuela Mulargia, Yahui Zhao, Raoul Manenti, Gentile Francesco Ficetola, Michael Veith
Data type: Dataset
Brief description: Detailed information on morphology and microclimate of the surveyed caves in the Monte Albo massif and number of observed individuals belonging to five predator species exploiting these caves. For spiders, the number of the observed cocoons is also reported. NA means that the data is not available.
Download file (483.48 kb)
